http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
김윤환,오장근,신향미,김영생,Kim, Yoon-Hwan,Oh, Jang-Gun,Shin, Hyang-Mi,Kim, Young-Saeng 대한두경부종양학회 2009 대한두경부 종양학회지 Vol.25 No.2
Dermoid cysts are benign neoplasm that is derived from both ectoderm and mesoderm. They may be found at various sites of the body, but are extremely rare to occur in the lower neck. We present the case of a 22-year old woman with a midline cystic mass anterior to the cervical trachea. The mass was excised under local anesthesia. Histopathologically the diagnosis was confirmed as a dermoid cyst.
김윤환,오장근,신향미,문태현,김정범,김영생,Kim, Yoon-Hwan,Oh, Jang-Gun,Shin, Hyang-Mi,Moon, Tae-Hyun,Kim, Jeong-Beom,Kim, Young-Saeng 대한기관식도과학회 2009 大韓氣管食道科學會誌 Vol.15 No.2
Myxoma is a benign mesenchymal neoplasm that can occur in the head and neck. Laryngeal myxoma is extremely rare and easily confused with a laryngeal polyp. The common clinical presentation is hoarseness, dysphonia, dyspnea and dysphagia depending on their size and location. Treatment for laryngeal myxoma is complete surgical excision with surrounding normal tissue. To our knowledge, 11 laryngeal myxomas have been reported in the English literature, and all patients except only 1 case were male. We report the second female case of myxoma on a vocal cord with a review of literature.
이종률(Jong Riul Lee),신향미(Hyang Mi Shin),최순정(Sun Jeong Choi) 대한외과학회 2010 Annals of Surgical Treatment and Research(ASRT) Vol.78 No.5
The most frequent tumor arising from retroperitoneum is sarcoma. Most sarcomas of retroperitoneal origin have no symptoms and comprise 15% of all sarcomas. However, they can grow so great as to cause pain, which implies the possibility of invasion to adjacent organs. Moreover, if its location is between right adrenal gland and inferior vena cava (IVC) ambiguity of its origin can arise. Leiomyosarcoma of IVC is so rare that it can be seen to mimic right adrenal tumor. This 56-year-old female patient with back pain since approximately 4 months prior was transferred to our hospital via local clinic. We performed radical resection of tumor including segmental resection of IVC. Final diagnosis was leiomyosarcoma of IVC. We report this case with a review of literature.
황찬하,강신택,김보현,변재용,정인호,신향미,김대중,Hwang, Chan-Ha,Kang, Shin-Taeg,Kim, Bo-Hyun,Byun, Jae-Yong,Jung, In-Ho,Shin, Hyang-Mi,Kim, Dae-Joong 대한족부족관절학회 2006 대한족부족관절학회지 Vol.10 No.1
Benign and malignant tumors are found in the foot, although the incidence is low. The most common bone tumor in the foot is osteochondroma, which is thought to develop in bones that form through the process of enchondral ossification. In particularly, osteochondromas in the foot mostly occur in metatarsal bones and phalanges. It is seldom found in talus. It is usually confused with osteophyte or enthesis. We report an osteochondroma case confirmed by roentgenographical and pathological investigation, after removing the masses form bilateral tali of a 19-year-old male patient presented with bilateral ankle joint pain for three years.
이종률(Jong Riul Lee),고병성(Beong Seong Ko),신향미(Hyang Mi Shin) 대한외과학회 2008 Annals of Surgical Treatment and Research(ASRT) Vol.74 No.4
The concern about multiple primary cancers has been raised in recent years, but their cause has yet to be elucidated clearly. It has been speculated that many factors may contribute, such as family history, genetic factors, chemotherapy, and radiotherapy.(1) The incidence of multiple primary cancers is estimated to be 13%. However, synchronous multiple primary cancers of the stomach and duodenum are uncommon due to the rarity of duodenal cancer. Duodenal cancer poses diagnostic difficulties because of its rarity, nonspecific signs and symptoms, and the fact that duodenum is usually ignored during upper gastrointestinal endoscopy. This 71-year-old female patient was diagnosed with double primary cancer of the stomach and duodenum, which was found by abdominal computed tomography preoperatively, and she underwent a Whipple procedure. The histological diagnosis revealed poorly-differentiated adenocarcinoma in the stomach and moderately-differentiated adenocarcinoma in the duodenum. Here we report a case of synchronous double primary cancer of the stomach and duodenum with a review of the literature.
강명진 ( Myung Jin Kang ),남궁경영 ( Kyung Young Namgung ),김미성 ( Mi Sung Kim ),고병성 ( Byung Sung Ko ),한창순 ( Chang Soon Han ),안현택 ( Hyun Taek Ahn ),신향미 ( Hyang Mi Shin ) 대한소화기학회 2004 대한소화기학회지 Vol.43 No.5
Kaposi`s sarcoma is a rare and slowly progressive disease that primarily affects the skin but has an associated visceral involvement. It can occur in the HIV-positive patients or patients treated with immunosuppressants. However, it is extremely rare in the patients receiving the treatment for inflammatory bowel disease. We used corticosteroid for the treatment of ulcerative colitis in 60-year-old woman. Then, Kaposis`s sarcoma occured in the skin and colon of the patient. Since she was HIV-negative, we believed that it was developed from the condition of corticosteroid-induced immunosuppression. We present a case of skin and colonic Kaposi`s sarcoma in a HIV-negative woman following treatment with corticosteroid for ulcerative colitis. (Korean J Gastroenterol 2004;43:316-319)
Yoon Hwan Kim(김윤환),Jang-Gun Oh(오장근),Hyang-Mi Shin(신향미),Young Saeng Kim(김영생) 대한두경부종양학회 2009 대한두경부 종양학회지 Vol.25 No.2
Dermoid cysts are benign neoplasm that is derived from both ectoderm and mesoderm. They may be found at various sites of the body, but are extremely rare to occur in the lower neck. We present the case of a 22-year old woman with a midline cystic mass anterior to the cervical trachea. The mass was excised under local anesthesia. Histopathologically the diagnosis was confirmed as a dermoid cyst.
신향미,성노현 충북대학교 의학연구소 2000 忠北醫大學術誌 Vol.10 No.2
융모막혈관종은 태반에서 발생하는 가장 흔한 양성 종양으로 대개는 크기가 작고 태반체 속에 묻혀 있으며 증상이 없기 때문에 발견되지 않는 경우가 많다. 그러나 드물게 종양이 큰 경우에는 태반의 태아면 또는 모체면쪽으로 돌출하며 양수과다, 조산 등을 나타낼 수 있다 한편 이 종양은 비교적 흔한 종양임에도 불구하고 그 기원세포는 명확히 밝혀지지 않았다. 저자들은 27세 경산부의 태반에서 조산의 원인이 된 장경 8 cm의 융모막혈관종 1예를 경험하고 cytokeratin 18과 CD34에 대한 항체를 이용한 면역조직화학검사로써 융모막혈관종은 융모막반과 고정융모의 혈관에서 기원했을 가능성을 밝혔다. Chorangioma is the most common benign tumor of the placenta. A case of unusually large chorangioma associated with premature delivery is presented. At 26 weeks of gestation, a 27-year-old woman delivered a female infant. The placenta weighed 650 gm and a large, solid mass, measuring 8 cm in diameter, was seen on fetal surface of the placenta protruding into amniotic cavity. Microscopically, the tumor was composed of numerous capillary-sized vessels separated by inconspicuous stroma. Immunohistochemically, tumor cells showed staining for CD34, vimentin, alpha smooth muscle (α-SM) actin and cytokeratin 18. The blood vessels within the chorionic plate and anchoring villi stained for cytokeratin 18, but the vasculature of the terminal villi lacked cytokeratins. In these results, the chorangioma originate most likely from blood vessels of the chorionic plate and anchoring villi.